Canonical Allele Identifier: CA2655998173
Gene: RASL10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29313139del , CM000684.2:g.29313139del GRCh38
NC_000022.10:g.29709128del , CM000684.1:g.29709128del GRCh37
NC_000022.9:g.28039128del NCBI36
NG_032959.1:g.11133del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216101.7:c.*165del MANE Select ENSP00000216101.6:n.*165del
ENST00000216101.6:c.*165del ENSP00000216101.6:n.*165del
ENST00000401450.3:c.*723del ENSP00000386095.3:n.*723del
NM_006477.4:c.*165del NP_006468.1:n.*165del
XM_011529821.1:c.*165del XP_011528123.1:n.*165del
XM_011529822.1:c.*165del XP_011528124.1:n.*165del
XM_011529823.1:c.*165del XP_011528125.1:n.*165del
NM_006477.5:c.*165del MANE Select NP_006468.1:n.*165del